Maria Lombardi

1.7k total citations
45 papers, 1.1k citations indexed

About

Maria Lombardi is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Maria Lombardi has authored 45 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 15 papers in Genetics and 10 papers in Surgery. Recurrent topics in Maria Lombardi's work include Lipoproteins and Cardiovascular Health (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Genetic and rare skin diseases. (5 papers). Maria Lombardi is often cited by papers focused on Lipoproteins and Cardiovascular Health (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Genetic and rare skin diseases. (5 papers). Maria Lombardi collaborates with scholars based in Netherlands, Italy and United States. Maria Lombardi's co-authors include Fulco van der Veen, Louis M. Havekes, Vincenzo Positano, Marcel M. A. M. Mannens, G.H. Westerveld, Sjoerd Repping, John J.P. Kastelein, Antonella Meloni, Anna Spasiano and Eliana Cracolici and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and Scientific Reports.

In The Last Decade

Maria Lombardi

42 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Maria Lombardi Netherlands 17 329 263 246 246 245 45 1.1k
S J Lauer United States 16 277 0.8× 74 0.3× 333 1.4× 141 0.6× 125 0.5× 20 947
Samad Barzegar United States 9 173 0.5× 88 0.3× 85 0.3× 141 0.6× 319 1.3× 11 810
Bhupinder Bharaj Canada 12 199 0.6× 83 0.3× 79 0.3× 40 0.2× 175 0.7× 20 589
Yvonne H. Datta United States 15 216 0.7× 73 0.3× 66 0.3× 218 0.9× 121 0.5× 24 982
Timothy Farren United Kingdom 9 440 1.3× 173 0.7× 111 0.5× 54 0.2× 61 0.2× 15 1.1k
James McRedmond Ireland 8 283 0.9× 46 0.2× 114 0.5× 174 0.7× 371 1.5× 9 977
Jean-Paul Beressi France 11 316 1.0× 75 0.3× 375 1.5× 71 0.3× 131 0.5× 20 1.2k
Panagiotis Flevaris United States 13 378 1.1× 33 0.1× 103 0.4× 194 0.8× 312 1.3× 14 930
Herbert Lau Canada 15 127 0.4× 58 0.2× 283 1.2× 198 0.8× 257 1.0× 37 849

Countries citing papers authored by Maria Lombardi

Since Specialization
Citations

This map shows the geographic impact of Maria Lombardi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Maria Lombardi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maria Lombardi more than expected).

Fields of papers citing papers by Maria Lombardi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maria Lombardi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Maria Lombardi. The network helps show where Maria Lombardi may publish in the future.

Co-authorship network of co-authors of Maria Lombardi

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Lombardi. A scholar is included among the top collaborators of Maria Lombardi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Maria Lombardi. Maria Lombardi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Maas, Saskia M., et al.. (2023). Should testing for mosaic genome-wide paternal uniparental disomy in Beckwith-Wiedemann spectrum (BWSp) be implemented in diagnostic testing?. European Journal of Human Genetics. 31(6). 615–616. 1 indexed citations
3.
Matà, Sabrina, Alessandro Barilaro, Maria Lombardi, et al.. (2023). Epidemiology of amyotrophic lateral sclerosis in the north east Tuscany in the 2018–2021 period. eNeurologicalSci. 31. 100457–100457. 1 indexed citations
4.
Foglieni, Chiara, Maria Lombardi, Davide Lazzeroni, et al.. (2022). Myosins and MyomiR Network in Patients with Obstructive Hypertrophic Cardiomyopathy. Biomedicines. 10(9). 2180–2180. 6 indexed citations
5.
6.
Lombardi, Maria, Davide Lazzeroni, Annalinda Pisano, et al.. (2020). Mitochondrial Energetics and Ca2+-Activated ATPase in Obstructive Hypertrophic Cardiomyopathy. Journal of Clinical Medicine. 9(6). 1799–1799. 13 indexed citations
7.
Mackay, Deborah, Jet Bliek, Maria Lombardi, et al.. (2019). Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes. Genetics Research. 101. e3–e3. 16 indexed citations
8.
Berry, Alessandra, Matteo Marconi, Flavia Chiarotti, et al.. (2019). Trehalose administration in C57BL/6N old mice affects healthspan improving motor learning and brain anti-oxidant defences in a sex-dependent fashion: a pilot study. Experimental Gerontology. 129. 110755–110755. 19 indexed citations
9.
Maza, A., et al.. (2017). Mosaic Focal Dermal Hypoplasia (Goltz Syndrome) in Two Female Patients. Acta Dermato Venereologica. 97(7). 853–854. 3 indexed citations
10.
Lombardi, Maria, Domenico Baccellieri, David Ferrara, et al.. (2017). P2X7 receptor antagonism modulates IL-1β and MMP9 in human atherosclerotic vessels. Scientific Reports. 7(1). 4872–4872. 29 indexed citations
11.
Lombardi, Maria, Saskia Bulk, Jacopo Celli, et al.. (2011). Mutation update for the PORCN gene. Human Mutation. 32(7). 723–728. 44 indexed citations
12.
Nannenberg, Eline A., Michelle Michels, Imke Christiaans, et al.. (2011). Mortality Risk of Untreated Myosin-Binding Protein C–Related Hypertrophic Cardiomyopathy. Journal of the American College of Cardiology. 58(23). 2406–2414. 16 indexed citations
13.
Todiere, Giancarlo, Danilo Neglia, Enza Fommei, et al.. (2011). Right ventricular remodelling in systemic hypertension: a cardiac MRI study. Heart. 97(15). 1257–1261. 32 indexed citations
14.
Maas, Saskia M., Maria Lombardi, A. J. van Essen, et al.. (2009). Phenotype and genotype in 17 patients with Goltz–Gorlin syndrome. Journal of Medical Genetics. 46(10). 716–720. 53 indexed citations
15.
Neglia, Danilo, et al.. (2008). Coronary microvascular dysfunction in hypertensive patients with left ventricular hypertrophy can be reversed by treatment with a fixed combination of perindropril and indapamide. European Heart Journal. 29. 103. 2 indexed citations
16.
17.
Westerveld, G.H., Sjoerd Repping, Maria Lombardi, & F. van der Veen. (2005). Mutations in the chromosome pairing gene FKBP6 are not a common cause of non-obstructive azoospermia. Molecular Human Reproduction. 11(9). 673–675. 13 indexed citations
18.
Lombardi, Maria, Joep C. Defesche, Sylvia W.A. Kamerling, et al.. (2000). Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in the Netherlands. Clinical Genetics. 57(2). 116–124. 47 indexed citations
19.
Sijbrands, Eric J.G., Rudi G. J. Westendorp, Maria Lombardi, et al.. (2000). Additional risk factors influence excess mortality in heterozygous familial hypercholesterolaemia. Atherosclerosis. 149(2). 421–425. 65 indexed citations
20.
Peeters, Armand V., Luc F. Van Gaal, L. du Plessis, et al.. (1997). Mutational and genetic origin of LDL receptor gene mutations detected in both Belgian and Dutch familial hypercholesterolemics. Human Genetics. 100(2). 266–270. 22 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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